Polymorphic microsatellites and Wilson disease (WD)

Wilson disease (WD), an autosomal recessive disorder of copper metabolism, has been previously mapped to chromosome 13q. Highly informative PCR-based polymorphic microsatellites closely linked to the WD locus (WND) at 13q14.3, as well as sequence-tagged sites for closely linked loci, are described....

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Stewart, E. A., White, A., Tomfohrde, J., Osborne-Lawrence, S., Prestridge, L., Bonne-Tamir, B., Scheinberg, I. H., George-Hyslop, P. St, Giagheddu, M., Kim, J.-W., Seo, J. K., Lo, W. H.-y., Ivanova-Smolenskaya, I. A., Limborska, S. A., Cavalli-Sforza, L. L., Farrer, L. A., Bowcock, A. M.
Format: Artigo
Idioma:Inglês
Publicat: 1993
Matèries:
Original Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682397/
https://ncbi.nlm.nih.gov/pubmed/8213814
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars